Dimethyl Sulfoxide (DMSO) Decreases Cell Proliferation and TNF-α, IFN-γ, and IL-2 Cytokines Production in Cultures of Peripheral Blood Lymphocytes
Dimethylsulfoxide (DMSO) is an amphipathic molecule composed of a polar domain characterized by the sulfinyl and two nonpolar methyl groups, for this reason it is able to solubilize polar and nonpolar substances and transpose hydrophobic barriers. DMSO is widely used to solubilize drugs of therapeut...
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Published in | Molecules (Basel, Switzerland) Vol. 22; no. 11; p. 1789 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
MDPI AG
10.11.2017
MDPI |
Subjects | |
Online Access | Get full text |
ISSN | 1420-3049 1420-3049 |
DOI | 10.3390/molecules22111789 |
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Abstract | Dimethylsulfoxide (DMSO) is an amphipathic molecule composed of a polar domain characterized by the sulfinyl and two nonpolar methyl groups, for this reason it is able to solubilize polar and nonpolar substances and transpose hydrophobic barriers. DMSO is widely used to solubilize drugs of therapeutic applications and studies indicated that 10% v/v concentration did not modify culture viability when used to treat human peripheral blood mononuclear cells (PBMC). However, some DMSO concentrations could influence lymphocyte activation and present anti-inflammatory effects. Therefore, the objective of this study was to evaluate the effect of DMSO on lymphocyte activation parameters. Cell viability analysis, proliferation, and cytokine production were performed on PBMC from six healthy subjects by flow cytometry. The results indicated that 2.5% v/v DMSO concentrations did not modify lymphocytes viability. DMSO at 1% and 2% v/v concentrations reduced the relative proliferation index of lymphocytes and at 5% and 10% v/v concentrations reduced the percentage of total lymphocytes, cluster of differentiation 4+ (CD4+) T lymphocytes and CD8+ T lymphocytes interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α) and interleukin-2 (IL-2) producers. Thus, it was concluded that DMSO has an in vitro anti-inflammatory effect by reducing lymphocyte activation demonstrated with proliferation reduction and the decrease of cytokine production. |
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AbstractList | Dimethylsulfoxide (DMSO) is an amphipathic molecule composed of a polar domain characterized by the sulfinyl and two nonpolar methyl groups, for this reason it is able to solubilize polar and nonpolar substances and transpose hydrophobic barriers. DMSO is widely used to solubilize drugs of therapeutic applications and studies indicated that 10% v/v concentration did not modify culture viability when used to treat human peripheral blood mononuclear cells (PBMC). However, some DMSO concentrations could influence lymphocyte activation and present anti-inflammatory effects. Therefore, the objective of this study was to evaluate the effect of DMSO on lymphocyte activation parameters. Cell viability analysis, proliferation, and cytokine production were performed on PBMC from six healthy subjects by flow cytometry. The results indicated that 2.5% v/v DMSO concentrations did not modify lymphocytes viability. DMSO at 1% and 2% v/v concentrations reduced the relative proliferation index of lymphocytes and at 5% and 10% v/v concentrations reduced the percentage of total lymphocytes, cluster of differentiation 4+ (CD4+) T lymphocytes and CD8+ T lymphocytes interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α) and interleukin-2 (IL-2) producers. Thus, it was concluded that DMSO has an in vitro anti-inflammatory effect by reducing lymphocyte activation demonstrated with proliferation reduction and the decrease of cytokine production. Dimethylsulfoxide (DMSO) is an amphipathic molecule composed of a polar domain characterized by the sulfinyl and two nonpolar methyl groups, for this reason it is able to solubilize polar and nonpolar substances and transpose hydrophobic barriers. DMSO is widely used to solubilize drugs of therapeutic applications and studies indicated that 10% concentration did not modify culture viability when used to treat human peripheral blood mononuclear cells (PBMC). However, some DMSO concentrations could influence lymphocyte activation and present anti-inflammatory effects. Therefore, the objective of this study was to evaluate the effect of DMSO on lymphocyte activation parameters. Cell viability analysis, proliferation, and cytokine production were performed on PBMC from six healthy subjects by flow cytometry. The results indicated that 2.5% DMSO concentrations did not modify lymphocytes viability. DMSO at 1% and 2% concentrations reduced the relative proliferation index of lymphocytes and at 5% and 10% concentrations reduced the percentage of total lymphocytes, cluster of differentiation 4⁺ (CD4⁺) T lymphocytes and CD8⁺ T lymphocytes interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α) and interleukin-2 (IL-2) producers. Thus, it was concluded that DMSO has an in vitro anti-inflammatory effect by reducing lymphocyte activation demonstrated with proliferation reduction and the decrease of cytokine production. Dimethylsulfoxide (DMSO) is an amphipathic molecule composed of a polar domain characterized by the sulfinyl and two nonpolar methyl groups, for this reason it is able to solubilize polar and nonpolar substances and transpose hydrophobic barriers. DMSO is widely used to solubilize drugs of therapeutic applications and studies indicated that 10% v/v concentration did not modify culture viability when used to treat human peripheral blood mononuclear cells (PBMC). However, some DMSO concentrations could influence lymphocyte activation and present anti-inflammatory effects. Therefore, the objective of this study was to evaluate the effect of DMSO on lymphocyte activation parameters. Cell viability analysis, proliferation, and cytokine production were performed on PBMC from six healthy subjects by flow cytometry. The results indicated that 2.5% v/v DMSO concentrations did not modify lymphocytes viability. DMSO at 1% and 2% v/v concentrations reduced the relative proliferation index of lymphocytes and at 5% and 10% v/v concentrations reduced the percentage of total lymphocytes, cluster of differentiation 4⁺ (CD4⁺) T lymphocytes and CD8⁺ T lymphocytes interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α) and interleukin-2 (IL-2) producers. Thus, it was concluded that DMSO has an in vitro anti-inflammatory effect by reducing lymphocyte activation demonstrated with proliferation reduction and the decrease of cytokine production.Dimethylsulfoxide (DMSO) is an amphipathic molecule composed of a polar domain characterized by the sulfinyl and two nonpolar methyl groups, for this reason it is able to solubilize polar and nonpolar substances and transpose hydrophobic barriers. DMSO is widely used to solubilize drugs of therapeutic applications and studies indicated that 10% v/v concentration did not modify culture viability when used to treat human peripheral blood mononuclear cells (PBMC). However, some DMSO concentrations could influence lymphocyte activation and present anti-inflammatory effects. Therefore, the objective of this study was to evaluate the effect of DMSO on lymphocyte activation parameters. Cell viability analysis, proliferation, and cytokine production were performed on PBMC from six healthy subjects by flow cytometry. The results indicated that 2.5% v/v DMSO concentrations did not modify lymphocytes viability. DMSO at 1% and 2% v/v concentrations reduced the relative proliferation index of lymphocytes and at 5% and 10% v/v concentrations reduced the percentage of total lymphocytes, cluster of differentiation 4⁺ (CD4⁺) T lymphocytes and CD8⁺ T lymphocytes interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α) and interleukin-2 (IL-2) producers. Thus, it was concluded that DMSO has an in vitro anti-inflammatory effect by reducing lymphocyte activation demonstrated with proliferation reduction and the decrease of cytokine production. |
Author | Dos Santos, Michaelle De Abreu Costa, Lucas Henrique Fernandes Ottoni, Marcelo Meireles, Agnes Alves de Avelar-Freitas, Bethânia Gomes de Almeida, Valéria De Fátima Pereira, Wagner Eustáquio Alvim Brito-Melo, Gustavo |
AuthorAffiliation | 3 Institute of Science and Technology, Federal University of the Jequitinhonha and Mucuri Valleys, Diamantina, MG 39100-000, Brazil 1 Immunology Laboratory, Integrated Center for Health Research, Federal University of the Jequitinhonha and Mucuri Valleys (UFVJM), Diamantina, MG 39100-000, Brazil; lucas.farmac@gmail.com (L.d.A.C.); m.ottoni@yahoo.com.br (M.H.F.O.); michaellegsantos@gmail.com (M.G.d.S.); agnesbm@gmail.com (A.B.M.); valeria.g.almeida@gmail.com (V.G.d.A.); wagnerufvjm@gmail.com (W.d.F.P.); gbrito1998@yahoo.com (G.E.A.B.-M.) 2 Multicenter Graduate Program in Physiological Sciences/UFVJM Graduate Program in Pharmaceutical Sciences/UFVJM, Federal University of the Jequitinhonha and Mucuri Valleys, Diamantina, MG 39100-000, Brazil 4 Graduate Program in Dentistry, School of Dentistry, Federal University of the Jequitinhonha and Mucuri Valleys, Diamantina, MG 39100-000, Brazil |
AuthorAffiliation_xml | – name: 3 Institute of Science and Technology, Federal University of the Jequitinhonha and Mucuri Valleys, Diamantina, MG 39100-000, Brazil – name: 2 Multicenter Graduate Program in Physiological Sciences/UFVJM Graduate Program in Pharmaceutical Sciences/UFVJM, Federal University of the Jequitinhonha and Mucuri Valleys, Diamantina, MG 39100-000, Brazil – name: 1 Immunology Laboratory, Integrated Center for Health Research, Federal University of the Jequitinhonha and Mucuri Valleys (UFVJM), Diamantina, MG 39100-000, Brazil; lucas.farmac@gmail.com (L.d.A.C.); m.ottoni@yahoo.com.br (M.H.F.O.); michaellegsantos@gmail.com (M.G.d.S.); agnesbm@gmail.com (A.B.M.); valeria.g.almeida@gmail.com (V.G.d.A.); wagnerufvjm@gmail.com (W.d.F.P.); gbrito1998@yahoo.com (G.E.A.B.-M.) – name: 4 Graduate Program in Dentistry, School of Dentistry, Federal University of the Jequitinhonha and Mucuri Valleys, Diamantina, MG 39100-000, Brazil |
Author_xml | – sequence: 1 givenname: Lucas surname: De Abreu Costa fullname: De Abreu Costa, Lucas – sequence: 2 givenname: Marcelo orcidid: 0000-0002-2333-2775 surname: Henrique Fernandes Ottoni fullname: Henrique Fernandes Ottoni, Marcelo – sequence: 3 givenname: Michaelle surname: Dos Santos fullname: Dos Santos, Michaelle – sequence: 4 givenname: Agnes surname: Meireles fullname: Meireles, Agnes – sequence: 5 givenname: Valéria surname: Gomes de Almeida fullname: Gomes de Almeida, Valéria – sequence: 6 givenname: Wagner surname: De Fátima Pereira fullname: De Fátima Pereira, Wagner – sequence: 7 givenname: Bethânia surname: Alves de Avelar-Freitas fullname: Alves de Avelar-Freitas, Bethânia – sequence: 8 givenname: Gustavo orcidid: 0000-0001-6138-7235 surname: Eustáquio Alvim Brito-Melo fullname: Eustáquio Alvim Brito-Melo, Gustavo |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29125561$$D View this record in MEDLINE/PubMed |
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Keywords | anti-inflammatory agents solvents dimethyl sulfoxide |
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SubjectTerms | anti-inflammatory agents Cell Death - drug effects Cell Proliferation - drug effects Cells, Cultured Cytokines dimethyl sulfoxide Dimethyl Sulfoxide - pharmacology Hemolysis - drug effects Humans Interferon-gamma - biosynthesis Interleukin-2 - biosynthesis Lymphocyte receptors Lymphocytes Lymphocytes - cytology Lymphocytes - drug effects Lymphocytes - metabolism solvents T cell receptors Tumor Necrosis Factor-alpha - biosynthesis Tumor necrosis factor-TNF |
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Title | Dimethyl Sulfoxide (DMSO) Decreases Cell Proliferation and TNF-α, IFN-γ, and IL-2 Cytokines Production in Cultures of Peripheral Blood Lymphocytes |
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